Bardoel AF - Search Results

1

Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients.

van Belzen MJ, Koeleman BP, Crusius JB, Meijer JW, Bardoel AF, Pearson PL, Sandkuijl LA, Houwen RH, Wijmenga C. van Belzen MJ, et al. Among authors: bardoel af. Genes Immun. 2004 May;5(3):215-20. doi: 10.1038/sj.gene.6364061. Genes Immun. 2004. PMID: 15014431

2

A major non-HLA locus in celiac disease maps to chromosome 19.

Van Belzen MJ, Meijer JW, Sandkuijl LA, Bardoel AF, Mulder CJ, Pearson PL, Houwen RH, Wijmenga C. Van Belzen MJ, et al. Among authors: bardoel af. Gastroenterology. 2003 Oct;125(4):1032-41. doi: 10.1016/s0016-5085(03)01205-8. Gastroenterology. 2003. PMID: 14517787

3

An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia.

Jungerius BJ, Hoogendoorn ML, Bakker SC, Van't Slot R, Bardoel AF, Ophoff RA, Wijmenga C, Kahn RS, Sinke RJ. Jungerius BJ, et al. Among authors: bardoel af. Mol Psychiatry. 2008 Nov;13(11):1060-8. doi: 10.1038/sj.mp.4002080. Epub 2007 Sep 25. Mol Psychiatry. 2008. PMID: 17893707

4

Genes and outcome after aneurysmal subarachnoid haemorrhage.

Ruigrok YM, Slooter AJ, Bardoel A, Frijns CJ, Rinkel GJ, Wijmenga C. Ruigrok YM, et al. J Neurol. 2005 Apr;252(4):417-22. doi: 10.1007/s00415-005-0661-y. Epub 2005 Feb 23. J Neurol. 2005. PMID: 15726267

5

Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families.

Heutink P, van Schothorst EM, van der Mey AG, Bardoel A, Breedveld G, Pertijs J, Sandkuijl LA, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Eur J Hum Genet. 1994;2(3):148-58. doi: 10.1159/000472358. Eur J Hum Genet. 1994. PMID: 7834274

6

Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma.

Devilee P, van Vliet M, Bardoel A, Kievits T, Kuipers-Dijkshoorn N, Pearson PL, Cornelisse CJ. Devilee P, et al. Cancer Res. 1991 Feb 1;51(3):1020-5. Cancer Res. 1991. PMID: 1670997

7

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

Heutink P, van der Mey AG, Sandkuijl LA, van Gils AP, Bardoel A, Breedveld GJ, van Vliet M, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Hum Mol Genet. 1992 Apr;1(1):7-10. doi: 10.1093/hmg/1.1.7. Hum Mol Genet. 1992. PMID: 1301144

8

Dutch patients with glycogen storage disease type II show common ancestry for the 525delT and del exon 18 mutations.

Ausems MG, ten Berg K, Sandkuijl LA, Kroos MA, Bardoel AF, Roumelioti KN, Reuser AJ, Sinke R, Wijmenga C. Ausems MG, et al. Among authors: bardoel af. J Med Genet. 2001 Aug;38(8):527-9. doi: 10.1136/jmg.38.8.527. J Med Genet. 2001. PMID: 11494962 Free PMC article. No abstract available.

9

Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17.

Bank RA, Robins SP, Wijmenga C, Breslau-Siderius LJ, Bardoel AF, van der Sluijs HA, Pruijs HE, TeKoppele JM. Bank RA, et al. Among authors: bardoel af. Proc Natl Acad Sci U S A. 1999 Feb 2;96(3):1054-8. doi: 10.1073/pnas.96.3.1054. Proc Natl Acad Sci U S A. 1999. PMID: 9927692 Free PMC article.

10

Identification of PLOD2 as telopeptide lysyl hydroxylase, an important enzyme in fibrosis.

van der Slot AJ, Zuurmond AM, Bardoel AF, Wijmenga C, Pruijs HE, Sillence DO, Brinckmann J, Abraham DJ, Black CM, Verzijl N, DeGroot J, Hanemaaijer R, TeKoppele JM, Huizinga TW, Bank RA. van der Slot AJ, et al. Among authors: bardoel af. J Biol Chem. 2003 Oct 17;278(42):40967-72. doi: 10.1074/jbc.M307380200. Epub 2003 Jul 24. J Biol Chem. 2003. PMID: 12881513 Free article.

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